Impacts of extending the π-conjugation of the 2,2′-biquinoline ligand on the photophysics and reverse saturable absorption of heteroleptic cationic iridium(iii) complexes

Author:

Lu Taotao1,Lu Cuifen12ORCID,Cui Peng134,Kilina Svetlana1,Sun Wenfang1ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, North Dakota State University, Fargo, ND 58108-6050, USA

2. Hubei Collaborative Innovation Center for Advanced Organochemical Materials & Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University, Wuhan, 430062, P. R. China

3. Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122, P. R. China

4. Materials and Nanotechnology Program, North Dakota State University, Fargo, ND 58108-6050, USA

Abstract

Extending the π-conjugation of the 2,2′-biquinoline ligand in Ir(iii) complexes via 7-benzothiazolylfluoren-2-yl substitution increased the triplet excited-state lifetime, leading to broad excited-state absorption at 480–800 nm and strong RSA at 532 nm.

Funder

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

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